Classifications

• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C3/00—Glass compositions
  • C03C3/04—Glass compositions containing silica
  • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
  • C03C3/097—Glass compositions containing silica with 40% to 90% silica, by weight containing phosphorus, niobium or tantalum
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C1/00—Ingredients generally applicable to manufacture of glasses, glazes, or vitreous enamels
  • C03C1/004—Refining agents
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C3/00—Glass compositions
  • C03C3/04—Glass compositions containing silica
  • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
  • C03C3/089—Glass compositions containing silica with 40% to 90% silica, by weight containing boron
  • C03C3/091—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium
  • C03C3/093—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium containing zinc or zirconium
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C3/00—Glass compositions
  • C03C3/04—Glass compositions containing silica
  • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
  • C03C3/095—Glass compositions containing silica with 40% to 90% silica, by weight containing rare earths
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C4/00—Compositions for glass with special properties
  • C03C4/20—Compositions for glass with special properties for chemical resistant glass
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
  • Y02E10/00—Energy generation through renewable energy sources
  • Y02E10/50—Photovoltaic [PV] energy

Definitions

• the present invention relates to a glass material, in particular to a glass material suitable for the field of photosensitive device packaging.
• photoelectric converters such as COMS and CCD apply glass materials for windows, so that the windows can play the role of light transmission and protection of photoelectric conversion chip.
• the earlier photosensitive devices such as COMS and CCD are usually placed in the camera with comfortable service environment, thus no high requirements are posed for chemical stability (acid resistance, water resistance, alkali resistance, etc.), weather resistance and temperature shock resistance of protective window of the photosensitive device.
• chemical stability ascid resistance, water resistance, alkali resistance, etc.
• weather resistance and temperature shock resistance of protective window of the photosensitive device.
• photosensitive devices require higher reliability under very harsh conditions.
• the photosensitive devices used in high-temperature fire need to withstand extreme temperature environments of 100-200°C or even higher; the photosensitive devices used for observation in marine environment need to be able to withstand long-term alkaline or acid erosion; the photosensitive devices used for observation of chemistry (chemical) experiment need to be able to withstand strong acid and alkali corrosion; the photosensitive devices used for on-board use and security need to be exposed to outdoor environment for a long time.
• the key component of the photosensitive chip is silicon single crystal, and the packaging housing is mainly made of ceramic material.
• the ceramic material enjoys excellent chemical stability and impact resistance performance, but its weakness lies in the optical opacity, thereby requiring brittle glass material as the light transmission window. In terms of chemical stability and thermal shock resistance, there is a massive gap between glass material and ceramic material.
• the best way to enhance the reliability of photosensitive devices in harsh external environment is to improve the chemical stability and temperature impact resistance of the window glass material.
• the glass material requires higher transmittance in the range of 360nm to 2000nm, in order to meet the needs of UV - visible light - near-infrared light sensitivity in different wavebands.
• the transmittance of glass material is usually subject to gradual increase from 360nm to 2000nm, so the lowest transmittance of glass can be characterized by the internal transmittance at 360nm ( ⁇ 360nm).
• ⁇ 360nm is above 78%, it represents that the packaged glass can meet the transmittance requirements of the above waveband. Since the glass for packaging needs to avoid reflection loss as much as possible, if the refractive index exceeds 1.60, the glass reflection loss will increase. Although the reflection loss can be reduced by coating anti-reflection film, it will result in cost increase and stray light interference problems.
• the technical problem to be solved by the present invention is to provide a glass material with high light transmittance and excellent chemical stability.
• the technical scheme of the present invention provides:
• the beneficial effects of the present invention are as follows: Through rational component design, the glass material of the present invention features high light transmittance and excellent chemical stability, so as to be able to be applied in the field of photosensitive device packaging.
• the glass material of the present invention is sometimes referred to as glass.
• the range of components of the glass material provided by the present invention will be described. If not specified herein, the content of each component and the total content are expressed in weight percentage relative to the total glass materials converted into oxide composition. "Converted into oxide composition” therein refers to that the total weight of this oxide is taken as 100% when the oxide, compound salt and hydroxide, used as raw materials for the composition of glass material of the present invention, are decomposed and transformed into oxides during melting.
• SiO 2 serves as a key component of the present glass.
• an appropriate amount of SiO 2 can ensure higher water resistance and acid resistance of the glass, and meanwhile achieve high light transmittance. If the content of SiO 2 is less than 50%, the water resistance, acid resistance and UV light transmittance of the glass are lower than the design requirements. If the content of SiO 2 is higher than 70%, the refractive index of the glass fails to meet the design requirements. The melting temperature of the glass will rise sharply, thus it is not easy to obtain high-quality glass during production, and the thermal expansion coefficient of the glass will decrease. Therefore, the content of SiO 2 in the present invention is confined to 50-70%, preferably 55-68%, and more preferably 60-68%.
• Adding an appropriate amount of B 2 O 3 into the glass can the transform the glass structure to be dense, improve the refractive index of the glass, and meanwhile achieve higher water and acid resistance. If the content thereof is less than 3%, the above effect is not obvious. If the content of B 2 O 3 is higher than 15%, the water and acid resistance of the glass will decrease. Therefore, the content of B 2 O 3 is confined to 3-15%, preferably more than 5% but less than or equal to 13%, more preferably 6-12%.
• the value of B 2 O 3 /SiO 2 affects the difficulty of glass production.
• B 2 O 3 /SiO 2 is less than 0.06, the melting temperature of the glass increases to aggravate the erosion of refractory materials, and it is easy to introduce more colored impurities and inclusions into the glass, resulting in that the transmittance of the glass fails to meet the design requirements. Meanwhile, the probability of defect increases within the product.
• B 2 O 3 /SiO 2 is more than 0.26, the melting temperature drop is not obvious, the erosion of B 2 O 3 on refractory materials increases, and it is easy to introduce more colored impurities and inclusions into the glass, resulting in that the short-wave transmittance of the glass fails to meet the design requirements. Meanwhile, the probability of defect increases on the product surface. Therefore, the value of B 2 O 3 /SiO 2 in the present invention is 0.06-0.26, preferably 0.08-0.2, more preferably 0.1-0.18.
• Adding an appropriate amount of Al 2 O 3 into the glass can improve the water and acid resistance of the glass, and meanwhile lower the thermal expansion coefficient of the glass, especially in the presence of alkali metal oxides. If the content of Al 2 O 3 is higher than 10%, the thermal expansion coefficient of the glass decreases rapidly, failing to meet the design requirements. Therefore, the content of Al 2 O 3 is confined to 0.5-10%, preferably 1-8%, more preferably 2-7%.
• Adding an appropriate amount of TiO 2 into the glass can enhance the refractive index of the glass, improve the water, acid and alkali resistance of the glass, and meanwhile reduce the thermal expansion coefficient of the glass and improve the thermal shock resistance of the glass. If the content of TiO 2 is less than 0.5%, the above effect is not obvious; if the content of TiO 2 exceeds 10%, the Abbe number of the glass is lower than the expected design value, and the short-wave transmittance decreases rapidly, especially under unstable melting atmosphere. More importantly, the high content of TiO 2 leads to a rapid rise in the refractive index of the glass, and the reflection loss of the short-wave wavelength increases in case of no anti-reflection film, resulting in further reduction of short-wave transmittance.
• the content of TiO 2 in the present invention is confined to 0.5-10%, preferably 1.5-8%.
• the content of TiO 2 is more preferably 2-7%.
• Adding ZnO, with large field strength in divalent metal oxides, into the glass can improve the acid, water and alkali resistance of the glass, enhance the refractive index of the glass, and meanwhile reduce the thermal expansion coefficient of the glass, especially in glass systems containing alkali metals.
• the content of ZnO is less than 1%, the above effect is not obvious.
• the content of ZnO exceeds 12%, the transition temperature of the glass decreases rapidly, so that the glass is easy to soften and deform under high-temperature working environment, exerting a fatal effect on glass devices that need to work at high temperature.
• the content thereof exceeds 12% the dispersion of the glass rises rapidly, and the Abbe number fails to meet the design requirements. Therefore, the content of ZnO is confined to 1-12%, preferably 2-10%, more preferably 3-8%.
• the value of (TiO 2 +ZnO)/Al 2 O 3 is more than 8.0, the UV transmittance of the glass decreases and the devitrification tendency increases; if the value of (TiO 2 +ZnO)/Al 2 O 3 is less than 0.5, the melting of glass reduces, the difficulty of bubble ejection increases and the inner quality becomes worse. Therefore, the value of (TiO 2 +ZnO)/Al 2 O 3 is 0.5-8.0, the value of (TiO 2 +ZnO)/Al 2 O 3 is preferably 0.7-7.0, and the value of (TiO 2 +ZnO)/Al 2 O 3 is more preferably 1.0-5.0.
• the value of ZnO/B 2 O 3 in the present invention is preferably 0.2-1.8, more preferably 0.3-1.0, and further preferably 0.4-0.8.
• Adding MgO, CaO, SrO and BaO, all belonging to alkaline-earth metal oxide, into the glass can enhance the refractive index and transition temperature of the glass, and adjust the stability and thermal expansion coefficient of the glass.
• the addition of alkaline-earth metal oxide leads to a rapid rise in Young's modulus of the glass.
• the devitrification resistance and chemical stability of the glass can be improved by making the ratio of alkaline-earth metal oxide to Al 2 O 3 ((MgO+CaO+SrO+BaO)/Al 2 O 3 ) to be below 1.0.
• (MgO+CaO+SrO+BaO)/Al 2 O 3 is preferably below 0.5, and (MgO+CaO+SrO+BaO)/Al 2 O 3 is more preferably below 0.2.
• the matching of optical system can be achieved with higher refractive index or higher transition temperature, which requires the addition of a small amount of alkaline-earth metal oxide.
• alkaline-earth metal oxide in order to avoid the rapid decline of water, acid and alkali resistance of the glass, it can be considered to add MgO, CaO, SrO and BaO separately in sequence or in combined form. If the individual content of alkaline-earth metal oxides such as MgO, CaO, SrO and BaO exceeds 5%, the devitrification resistance performance of the glass will decline rapidly, so that it is not easy to obtain large-caliber high-quality products. Therefore, the content of MgO, CaO, SrO and BaO is confined to be below 5% respectively, preferably below 3%, more preferably below 2%.
• Li 2 O, Na 2 O and K 2 O belong to alkali metal oxides.
• the content thereof is closely related to the thermal expansion coefficient, chemical stability and internal quality of the glass.
• Adding Li 2 O into the glass can lower the glass melting temperature and enhance the bubble degree of the glass. At the same time, compared with the other two alkali metal oxides, it brings the minimum loss to chemical stability of the glass.
• the content of Li 2 O exceeds 5%, the curing speed of the glass is slow during the forming process (namely, the process of glass liquid from liquid cooling to solid state), which is unfavorable for the production of large-size high-quality products (in case of manufacturing of products with width or diameter of more than 340mm and thickness of more than 40mm, it is easy to have unqualified stripe degree and internal devitrification).
• the content of Li 2 O is confined to be below 5%, preferably below 3%, more preferably 0%.
• the total content of Na 2 O and K 2 O (Na 2 O+K 2 O) exceeds 22%, the Abbe number of the glass is lower than the design requirements, and the thermal expansion coefficient of the glass exceeds the design requirements. Meanwhile, the dielectric constant of the glass rises rapidly, leading to a rapid decline in the insulation performance of the glass, which is unfavorable for certain applications requiring insulation.
• Na 2 O+K 2 O is less than 5%, the thermal expansion coefficient of the glass fails to meet the design requirements, and meanwhile, the coloring ability of the variable components in the glass will be enhanced, and the short-wave transmittance of the glass fails to meet the design requirements. Therefore, the total content of Na 2 O and K 2 O (Na 2 O+K 2 O) is 5-22%, preferably 6-20%, more preferably 8-18%.
• Adding Na 2 O into the glass can significantly increase the thermal expansion coefficient of the glass, and meanwhile reduce the high-temperature viscosity of the glass, so that it is easier to obtain glass products, with a width of more than 330mm, that can be processed into 12-inch packaging wafers.
• the content of Na 2 O exceeds 12%, the refractive index of the glass decreases and the chemical stability of the glass decreases rapidly, which cannot meet the design requirements.
• the content of Na 2 O is less than 2%, the thermal expansion coefficient of the glass fails to meet the design requirements, and meanwhile the chemical stability deteriorates seriously. Therefore, the content of Na 2 O is confined to 2-12%, preferably 3-10%, more preferably 4-9%.
• Adding an appropriate amount of K 2 O into the glass can enhance the thermal expansion coefficient of the glass, reduce the high-temperature viscosity of the glass and enhance the bubble degree of the glass, especially under the coexistence with Na 2 O. Adding an appropriate amount of K 2 O into the glass will not obviously damage the chemical stability of the glass. However, if the content thereof exceeds 12%, the water, acid and alkali resistance of the glass deteriorates. If the content of K 2 O is less than 2%, the effect of increasing thermal expansion coefficient and reducing high-temperature viscosity is not obvious. Therefore, the content of K 2 O is confined to 2-12%, preferably 3-10%, more preferably 4-9%.
• the value of (B 2 O 3 +K 2 O)/Al 2 O 3 is more than 10.0, the alkali resistance of the glass decreases and the thermal expansion coefficient increases; if the value of (B 2 O 3 +K 2 O)/Al 2 O 3 is less than 1.0, the melting of the glass reduces and the transition temperature increases. Therefore, the value of (B 2 O 3 +K 2 O)/Al 2 O 3 is preferably 1.0-10.0, the value of (B 2 O 3 +K 2 O)/Al 2 O 3 is more preferably 1.5-8.0, and the value of (B 2 O 3 +K 2 O)/Al 2 O 3 is further preferably 2.0-6.0.
• the value of (Na 2 O+K 2 O)/(B 2 O 3 +ZnO) is less than 0.2, the free oxygen is insufficient in the glass system, resulting in a decrease in the probability of components such as B 2 O 3 and ZnO entering the glass network and a sharp decrease in chemical stability, and meanwhile, the expansion coefficient of the glass is reduced, which cannot meet the design requirements.
• the value of (Na 2 O+K 2 O)/(B 2 O 3 +ZnO) is more than 2.5, the free oxygen in the glass system is excessive, leading to a sharp decline in the chemical stability of the glass and glass expansion coefficient beyond the design requirements. Therefore, when the value of (Na 2 O+K 2 O)/(B 2 O 3 +ZnO) is 0.2-2.5, preferably 0.3-2.0, more preferably 0.5-1.5, the chemical stability and thermal expansion coefficient of the glass are the most balanced.
• alkaline-earth metal oxides such as MgO, CaO, SrO and BaO into the glass is more favorable to the improvement of chemical stability than alkali metal oxides such as Li 2 O, Na 2 O and K 2 O.
• the value of (SiO 2 +TiO 2 )/(Na 2 O+ZnO) is more than 12.0, the glass becomes difficult to melt and clarify, and it is difficult to remove bubbles and inclusions inside the glass. Thus, it is difficult to obtain the glass with bubble degree above Grade A 0 , and inner stripes of the glass are serious. If the value of (SiO 2 +TiO 2 )/(Na 2 O+ZnO) is less than 3.0, the thermal expansion coefficient of the glass decreases rapidly, which is beyond the design requirements. Therefore, the value of (SiO 2 +TiO 2 )/(Na 2 O+ZnO) is preferably controlled to be 3.0-12.0, more preferably 3.0-10.0, further preferably 4.0-8.0.
• Adding an appropriate amount of ZrO 2 into the glass can improve the chemical stability and thermal shock resistance of the glass, and meanwhile enhance the refractive index of the glass. However, it is characterized by an obvious increase in the melting temperature of the glass. If the content thereof is higher than 5%, the glass is prone to inclusion defect. Therefore, the content of ZrO 2 is confined to be below 5%, preferably below 3%. In some implementations, when the chemical stability and strength of the glass are abundant, ZrO 2 is preferably to be not added.
• Adding an appropriate amount of P 2 O 5 into the glass can increase the strength of the glass, especially when chemical strengthening is required. However, if the content thereof exceeds 5%, the differential phase is easy to produce inside the glass, and the molding temperature of the glass is greatly increased. Therefore, the content of P 2 O 5 is confined to 0-5%, preferably 0-3%. In some implementations, when the glass strength design meets the use requirements, P 2 O 5 is preferably to be not added.
• an appropriate amount of oxides such as La 2 O 3 , Y 2 O 3 , Gd 2 O 3 , Nb 2 O 5 and WO 3 can be added.
• the individual or combined content thereof exceeds 5%, the Young's modulus of the glass rises rapidly. Although the strength of the glass rises, the brittleness of the glass rises faster and the thermal shock resistance decreases. In addition, the devitrification resistance performance and short-wave transmittance of the glass will deteriorate.
• the content of La 2 O 3 , Y 2 O 3 , Gd 2 O 3 , Nb 2 O 5 and WO 3 is below 5% respectively, preferably below 3%, more preferably below 1%, further preferably 0%. Furthermore, the total content of La 2 O 3 , Y 2 O 3 , Gd 2 O 3 , Nb 2 O 5 and WO 3 is preferably below 5%, more preferably below 3%, further preferably below 1%.
• the clarifying effect of the glass can be improved by adding one or more components of 0-1% of Sb 2 O 3 , SnO 2 , SnO, NaCl, sulfate and CeO 2 , preferably using Sb 2 O 3 as a clarifying agent, preferably adding 0-0.5% of the clarifying agent.
• Adding F into the glass can increase the volatilization of the glass raw material and is easy to cause environmental pollution and deterioration of the glass stripe degree, and thus F is preferred to be not contained in the glass of the present invention.
• Adding Ta 2 O 5 into the glass will greatly increase the refractive index and cost of the glass and worsen the melting performance of the glass, and thus Ta 2 O 5 is preferred to be not contained in the glass of the present invention.
• Th, Cd, Tl, Os, Be and Se oxides have been used in a controlled manner as a harmful chemical substance in recent years, which is necessary not only in the glass manufacturing process, but also in the processing procedure and disposal after the productization for environmental protection measures. Therefore, in the case of attaching importance to the influence on the environment, it is preferably not actually included except for the inevitable incorporation. As a result, the glass does not actually contain a substance that contaminates the environment. Therefore, the glass of the present invention can be manufactured, processed, and discarded even if no measure is taken as a special environmental countermeasure.
• As 2 O 3 and PbO are not contained in the glass of the present invention.
• As 2 O 3 can eliminate bubbles and better prevent glass from coloring, the addition of As 2 O 3 will increase the platinum erosion of glass on the furnace, especially on the platinum furnace, resulting in more platinum ions entering the glass. It brings a negative impact on the service life of the platinum furnace.
• PbO can significantly improve the high refractive index and high dispersion performance of the glass, but both PbO and As 2 O 3 cause environmental pollution.
• not containing means that the compound, molecule or element and the like are not intentionally added to the glass of the present invention as raw materials; however, as raw materials and/or equipment for the production of glass, there will be some impurities or components that are not intentionally added in small or trace amounts in the final glass, and this situation also falls within the protection scope of the present invention patent.
• the refractive index (nd) and Abbe number (v d ) of the glass material are measured as per the method specified in GB/T 7962.1-2010 .
• the lower limit of refractive index (nd) is 1.48, preferably 1.50, more preferably 1.51; the upper limit of refractive index (nd) is 1.56, preferably 1.55, more preferably 1.54; the lower limit of Abbe number (v d ) is 50, preferably 51, more preferably 53; the upper limit of Abbe number (v d ) is 58, preferably 57, more preferably 56.
• the acid resistance stability (D A ) (powder method) of the glass material is tested as per the method specified in GB/T 17129 .
• the acid resistance stability herein is sometimes referred to as acid resistance or acid resistance stability.
• the acid resistance stability (D A ) of the glass material provided by the present invention is above Class 2, preferably Class 1.
• the water resistance stability (D W ) (powder method) of the glass material is tested as per the method specified in GB/T 17129 .
• the water resistance stability herein is sometimes referred to as water resistance or water resistance stability.
• the water resistance stability (D W ) of the glass material provided by the present invention is above Class 2, preferably Class 1.
• the alkali resistance stability of the glass material is tested in accordance with the test conditions and requirements of ISO 10629.
• the alkali resistance stability herein is sometimes referred to as alkali resistance or alkali resistance stability.
• the glass into 30mm ⁇ 30mm ⁇ 2mm test samples, polish them on six sides, and place into 2000ml of NaOH solution.
• concentration of the NaOH solution is 0.01mol/L
• PH value is 12.0.
• the PH value change of the test solution is monitored by a PH meter at regular intervals, and the reaction test solution is replaced in time.
• the weight loss of the sample represented by mg, is measured by an electronic balance.
• the weight loss of the glass material provided by the present invention, after the test in accordance with the above method, is less than 9mg, preferably less than 7mg, more preferably less than 5mg.
• the thermal expansion coefficient mentioned in the present invention refers to the average expansion coefficient of the glass at 20-300°C, which is represented by ⁇ 20-300°C and tested in accordance with the method specified in GB/T7962.16-2010 .
• the upper limit of the average thermal expansion coefficient ( ⁇ 20-300°C ) is 90 ⁇ 10 -7 /K, preferably 85 ⁇ 10 -7 /K, more preferably 80 ⁇ 10 -7 /K;
• the lower limit of the average thermal expansion coefficient ( ⁇ 20-300°C ) is 60 ⁇ 10 -7 /K, preferably 65 ⁇ 10 -7 /K, more preferably 68 ⁇ 10 -7 /K.
• the light transmittance mentioned in the present invention refers to the light transmittance of 10mm-thick glass sample at 360nm, which is represented by ⁇ 360nm and tested in accordance with the method specified in GBAT7962.12-2010.
• the internal transmittance at 360nm ( ⁇ 360nm ) of the glass material provided by the present invention is above 78%, preferably above 82%, more preferably above 85%.
• T g The Transition temperature (T g ) of the glass is tested according to the method specified in GBAT7962.16-2010.
• the upper limit of transition temperature (T g ) of the glass provided by the present invention is 610°C, preferably 600°C, more preferably 580°C; the lower limit of the transition temperature (T g ) is 500°C, preferably 520°C, more preferably 530°C.
• the lower limit of Young's modulus (E) is 6000 ⁇ 10 7 Pa, preferably 6500 ⁇ 10 7 Pa, more preferably 7000 ⁇ 10 7 Pa; the upper limit of Young's modulus (E) is 8500 ⁇ 10 7 Pa, preferably 8000 ⁇ 10 7 Pa.
• the bubble degree of the glass material is tested as per the test method specified in GB/T7962.8-2010 .
• the bubble degree of the glass material provided by the present invention is above Grade A, preferably above Grade A 0 , more preferably Grade A 00 .
• the stripe degree of the glass material is measured as per the method specified in MLL-G-174B.
• the method is to use a stripe meter, composed of point light source and lens, to compare and check the standard sample from the direction where the stripes are most easily seen. It can be divided into 4 levels, i.e., Grades A, B, C and D. Grade A refers to that no visible stripes can be seen under the specified detection conditions, Grade B refers to that fine and scattered stripes can be seen under the specified detection conditions, Grade C refers to that slight parallel stripes can be seen under the specified detection conditions, and Grade D refers to that rough stripes can be seen under the specified detection conditions.
• the stripe degree of the glass material provided by the present invention is above Grade C, preferably above Grade B.
• the glass material of the present invention can be widely used in the packaging field of electronic devices and photosensitive devices, and can also be used in the manufacture of glass elements and various equipment or instruments, such as imaging device, sensor, microscope, medical technology, digital projection, communication, optical communication technology/information transmission, optics/lighting in the automobile field, photolithography, excimer laser, wafer, computer chip, and integrated circuit and electronic device including such circuit and chip, or camera equipment and device used in the fields of on-board product, surveillance and security.
• imaging device such as imaging device, sensor, microscope, medical technology, digital projection, communication, optical communication technology/information transmission, optics/lighting in the automobile field, photolithography, excimer laser, wafer, computer chip, and integrated circuit and electronic device including such circuit and chip, or camera equipment and device used in the fields of on-board product, surveillance and security.
• the manufacturing method of the glass material provided by the present invention is as follows:
• the glass of the present invention is made of conventional raw materials with conventional process.
• Those skilled in the art can appropriately select raw materials, process methods and process parameters according to actual needs.
• This embodiment obtains the glass material with the composition shown in Tables 1 to 2 by the above manufacturing method of glass material.
• the characteristics of each glass are measured by the test method described in the present invention, and the measurement results are shown in Tables 1 to 2.
• Table 1 Component (wt%) 1# 2# 3# 4# 5# 6# 7# 8# 9# SiO 2 64.1 63.6 59.9 53.6 55.8 63.2 63 61.8 50.1 B 2 O 3 8.2 8.2 7.5 13.3 7.8 8.1 6 7.9 9.7 Al 2 O 3 4.1 4.7 4.7 4.6 12 5.4 7.7 6.2 4.2 P 2 O 5 0 0 0 0 0 0 1.1 0 0 0 0 La 2 O 3 0 0 0 0 0 0 0 0 0 4.5 Y 2 O 3 0 0 0 0 0 0 0 0 0 Gd 2 O 3 0 0 0 0 0 0 0 0 5 TiO 2 4.3 4.2

Landscapes

• Chemical & Material Sciences (AREA)
• General Chemical & Material Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Geochemistry & Mineralogy (AREA)
• Materials Engineering (AREA)
• Organic Chemistry (AREA)
• Ceramic Engineering (AREA)
• Glass Compositions (AREA)

Applications Claiming Priority (2)

Publications (2)

Family

ID=71553125

Family Applications (1)

Country Status (6)

Families Citing this family (17)

Family Cites Families (34)

• 2020
  • 2020-05-27 CN CN202010460020.2A patent/CN111423111B/zh active Active
• 2021
  • 2021-04-14 US US17/923,675 patent/US20230174409A1/en active Pending
  • 2021-04-14 WO PCT/CN2021/087203 patent/WO2021238476A1/fr not_active Ceased
  • 2021-04-14 JP JP2022572544A patent/JP2023528338A/ja active Pending
  • 2021-04-14 EP EP21811829.7A patent/EP4159696A4/fr active Pending
  • 2021-04-21 TW TW110114261A patent/TWI756113B/zh active
• 2025
  • 2025-03-10 JP JP2025037346A patent/JP2025087872A/ja active Pending

Also Published As

Similar Documents

Legal Events